Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7080536
rs7080536
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.040 1.000 4 2016 2018
dbSNP: rs11575688
rs11575688
0.925 0.080 10 113583298 missense variant G/C snv 1.0E-02 1.1E-02
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2286742
rs2286742
1.000 0.080 10 113580733 intron variant G/A;C snv 0.57; 8.2E-06
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs3740530
rs3740530
1.000 0.080 10 113574365 synonymous variant C/T snv 0.63 0.55
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2019 2019